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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954825Generated: November 3, 2026

Triethylamine → HCID 22082760, compound

https://huagongshe.com/reaction/1954825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
ReactantHCID 54282228HCID 54282228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
ProductHCID 22082760HCID 22082760—

Reaction Steps

α,α,α-Trifluoro-p-toluic acid (0.15 g, 0.8 mmol) was suspended in thionyl chloride (3 mL) and refluxed for 30 minutes (everything dissolved after a few minutes). The excess of thionyl chloride was removed in vacuo with toluene. The residue was dissolved in methylene chloride (5 mL) and added dropwise to an ice cold solution of (R)-2-amino-8-(1-methylpiperidin-4-yl)-1,2,3,4-tetrahydronaphthalene (0.15 g, 0.6 mmol) and triethylamine (92 mg, 0.9 mmol) in methylene chloride (5 mL). The mixture was stirred for 15 minutes and was then diluted with ethyl acetate, washed with ammonia (2 M) and dried (MgSO4). The solvent was removed in vacuo. The residue was purified by flash chromatography on silica gel using methylene chloride/ethanol 5:1, containing 0.5% of ammonia, as the eluent. The title compound was obtained as off-white crystals. Yield 140 mg (55%): mp 163-166° C.; [α]21D +36° (c 0.5, CHCl3); EIMS (70 eV) m/z (relative intensity) 416 (48, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124283
Source datasetuspto-grants-2000_09
ORD IDord-8b0acea5a4a849b9a924083c3f335640
Source noteuspto-grants-2000_09